ATE405289T1 - 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES - Google Patents
6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVESInfo
- Publication number
- ATE405289T1 ATE405289T1 AT02793421T AT02793421T ATE405289T1 AT E405289 T1 ATE405289 T1 AT E405289T1 AT 02793421 T AT02793421 T AT 02793421T AT 02793421 T AT02793421 T AT 02793421T AT E405289 T1 ATE405289 T1 AT E405289T1
- Authority
- AT
- Austria
- Prior art keywords
- group
- alkoxy
- represent
- fluorobicyclo
- different
- Prior art date
Links
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 title 1
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 abstract 1
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 230000003042 antagnostic effect Effects 0.000 abstract 1
- 230000001430 anti-depressive effect Effects 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
- A61K31/198—Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/46—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C229/50—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms being part of the same condensed ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/24—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
- C07C237/26—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton of a ring being part of a condensed ring system formed by at least four rings, e.g. tetracycline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/18—All rings being cycloaliphatic the ring system containing six carbon atoms
Abstract
An antidepressant comprising, as an active ingredient, a compound having an antagonistic effect on group II metabotropic glutamate receptors, as well as a 2-amino-3-alkoxy-6-fluoro-bicycloÄ3.1.0Ühexane-2,6-dicarboxylic acid derivative of Formula ÄIÜ: <CHEM> Äwherein R<1> and R<2>, which may be the same or different, each represent a hydroxyl group, a C1-10 alkoxy group, etc.; R<3> represents a C1-10 acyl group, a C1-6 alkoxy-C1-6 acyl group, etc.; and R<4> and R<5>, which may be the same or different, each represent a hydrogen atom, a C1-10 alkyl group, etc.Ü or a pharmaceutically acceptable salt or hydrate thereof.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001395797 | 2001-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE405289T1 true ATE405289T1 (en) | 2008-09-15 |
Family
ID=27602080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT02793421T ATE405289T1 (en) | 2001-12-27 | 2002-12-26 | 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES |
Country Status (24)
Country | Link |
---|---|
US (1) | US7157594B2 (en) |
EP (1) | EP1459765B1 (en) |
JP (1) | JP4230919B2 (en) |
KR (2) | KR100897970B1 (en) |
CN (1) | CN1281274C (en) |
AT (1) | ATE405289T1 (en) |
AU (1) | AU2002359923B2 (en) |
BR (1) | BR0215462A (en) |
CA (1) | CA2471642C (en) |
CY (1) | CY1108380T1 (en) |
DE (1) | DE60228491D1 (en) |
DK (1) | DK1459765T3 (en) |
ES (1) | ES2311642T3 (en) |
HK (1) | HK1073258A1 (en) |
HU (1) | HU228436B1 (en) |
MX (1) | MXPA04006322A (en) |
NO (1) | NO328844B1 (en) |
NZ (1) | NZ533699A (en) |
PL (1) | PL208123B1 (en) |
PT (1) | PT1459765E (en) |
RU (1) | RU2315622C2 (en) |
SI (1) | SI1459765T1 (en) |
WO (1) | WO2003061698A1 (en) |
ZA (2) | ZA200404795B (en) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA03003690A (en) * | 2000-10-27 | 2004-05-05 | Chiron Spa | Nucleic acids and proteins from streptococcus groups a b. |
PT1517915E (en) * | 2002-06-11 | 2009-04-09 | Lilly Co Eli | Prodrugs of excitatory amino acids |
US7109383B2 (en) * | 2002-09-27 | 2006-09-19 | Central Glass Company, Limited | Fluorine-containing allyl ether compounds, their copolymers, and resist compositions and anti-reflection film materials using such copolymers |
NZ580554A (en) | 2003-06-26 | 2011-01-28 | Taisho Pharmaceutical Co Ltd | 2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic ester derivative |
JP5485492B2 (en) * | 2004-12-15 | 2014-05-07 | 大正製薬株式会社 | Drugs for the prevention and treatment of depression |
EP2258359A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation with sabcomelin |
JP2009506069A (en) | 2005-08-26 | 2009-02-12 | ブレインセルス,インコーポレイティド | Neurogenesis through modulation of muscarinic receptors |
AU2006304787A1 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by PDE inhibition |
CA2625210A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
AR059898A1 (en) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | DERIVATIVES OF 3-CIANO-PIRIDONA 1,4-DISUSTITUTED AND ITS USE AS ALLOSTERIC MODULATORS OF MGLUR2 RECEIVERS |
EP2026813A2 (en) | 2006-05-09 | 2009-02-25 | Braincells, Inc. | 5 ht receptor mediated neurogenesis |
EP2377531A2 (en) | 2006-05-09 | 2011-10-19 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
US7998971B2 (en) | 2006-09-08 | 2011-08-16 | Braincells Inc. | Combinations containing a 4-acylaminopyridine derivative |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
CN101801951B (en) | 2007-09-14 | 2013-11-13 | 杨森制药有限公司 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones |
KR20100065191A (en) | 2007-09-14 | 2010-06-15 | 오르토-맥닐-얀센 파마슈티칼스 인코포레이티드 | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
TW200927731A (en) | 2007-09-14 | 2009-07-01 | Ortho Mcneil Janssen Pharm | 1,3-disubstituted-4-phenyl-1H-pyridin-2-ones |
ES2637794T3 (en) | 2007-11-14 | 2017-10-17 | Janssen Pharmaceuticals, Inc. | Imidazo [1,2-A] pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors |
RU2510396C2 (en) | 2008-09-02 | 2014-03-27 | Янссен Фармасьютикалз, Инк. | 3-azabicyclo[3,1,0]hexyl derivatives as modulators of metabotropic glutamate receptors |
BRPI0920354A2 (en) | 2008-10-16 | 2017-06-27 | Addex Pharmaceuticals Sa | indole and benzomorpholine derivatives as metabotropic glutamate receptor modulators |
AU2009319387B2 (en) | 2008-11-28 | 2012-05-10 | Addex Pharma S.A. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
RS53075B (en) | 2009-05-12 | 2014-04-30 | Janssen Pharmaceuticals Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
JP5707390B2 (en) | 2009-05-12 | 2015-04-30 | ジャンセン ファーマシューティカルズ, インコーポレイテッド | 1,2,4-Triazolo [4,3-a] pyridine derivatives and their use as positive allosteric modulators of the mGluR2 receptor |
EP2502897B1 (en) | 2009-11-18 | 2014-07-09 | Taisho Pharmaceutical Co., Ltd. | Method for producing optically active bicyclo [3.1.0]hexane derivative using enzyme |
TW201124372A (en) | 2009-11-19 | 2011-07-16 | Taisho Pharmaceutical Co Ltd | Process for producing 3-alkoxy-2-amino-6-fluorobicyclo[310]hexane-2,6-dicarboxylic acid derivative and intermediate thereof |
EP2661435B1 (en) | 2010-11-08 | 2015-08-19 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
EP2649069B1 (en) | 2010-11-08 | 2015-08-26 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
EP2643320B1 (en) | 2010-11-08 | 2015-03-04 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
AR083845A1 (en) | 2010-11-18 | 2013-03-27 | Lilly Co Eli | 3-PHENYLSULPHANYLME-BICYCLE COMPOUNDS [3.1.0] HEXANE 4-REPLACED AS ANTAGONISTS OF mGluR2 / 3 |
WO2012068041A1 (en) | 2010-11-18 | 2012-05-24 | Eli Lilly And Company | 4-SUBSTITUTED-3-BENZYLOXY-BICYCLO[3.1.0]HEXANE COMPOUNDS AS mGluR 2/3 ANTAGONISTS |
PT2721012T (en) | 2011-06-17 | 2016-07-27 | Lilly Co Eli | Bicyclo(3.1.0)hexane-2,6-dicarboxylic acid derivatives as mglu2 receptor agonist |
WO2013062680A1 (en) * | 2011-10-25 | 2013-05-02 | Braincells, Inc. | Novel compounds and compositions thereof for treating nervous system disorders |
RU2496495C2 (en) * | 2011-12-05 | 2013-10-27 | Учреждение Российской академии медицинских наук Научно-исследовательский институт нормальной физиологии имени П.К. Анохина РАМН | USING SELECTIVE ANTAGONIST OF GLUAMATE RECEPTOR Ro-256981 FOR TARGETED EFFECT ON COGNITIVE FUNCTIONS |
SG11201407973SA (en) * | 2012-06-01 | 2015-01-29 | Taisho Pharmaceutical Co Ltd | Prodrug of fluorine-containing amino acid |
JO3368B1 (en) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
JO3367B1 (en) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
DK3431106T3 (en) | 2014-01-21 | 2021-03-15 | Janssen Pharmaceutica Nv | COMBINATIONS INCLUDING POSITIVE ALLOSTERIC MODULATORS OR ORTHOSTERIC AGONISTS OF METABOTROP GLUTAMATERG SUBTYPE 2 RECEPTOR AND USE OF THESE |
ES2860298T3 (en) | 2014-01-21 | 2021-10-04 | Janssen Pharmaceutica Nv | Combinations comprising positive allosteric modulators of metabotropic glutamatergic receptor subtype 2 and their use |
DK3445743T3 (en) | 2016-04-18 | 2021-10-18 | Taisho Pharmaceutical Co Ltd | PRODUCT OF AMINO ACID DERIVATIVE |
JP7314494B2 (en) * | 2017-10-17 | 2023-07-26 | 大正製薬株式会社 | Pharmaceuticals containing prodrugs of amino acid derivatives |
KR20220062838A (en) | 2020-11-09 | 2022-05-17 | 대우조선해양 주식회사 | Full spade rudder and ship having the same |
JP2024004505A (en) * | 2020-11-26 | 2024-01-17 | 大正製薬株式会社 | Method for producing amino acid derivative |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA000894B1 (en) | 1995-11-16 | 2000-06-26 | Эли Лилли Энд Компани | substituted bicyclohexanecarboxylic acids and derivatives thereof as excitatory amino acid receptor antagonists, method for producing and use thereof |
ZA969485B (en) * | 1995-11-16 | 1998-05-12 | Lilly Co Eli | Excitatory amino acid receptor antagonists. |
ZA983930B (en) * | 1997-05-14 | 1999-11-08 | Lilly Co Eli | Excitatory amino acid receptor modulators. |
ATE269293T1 (en) | 1998-08-31 | 2004-07-15 | Taisho Pharmaceutical Co Ltd | 6-FLUORO(3.1.0)HEXANE DERIVATIVES |
JP4194715B2 (en) | 1998-08-31 | 2008-12-10 | 大正製薬株式会社 | 6-Fluorobicyclo [3.1.0] hexane derivative |
CH694053A5 (en) | 1998-09-03 | 2004-06-30 | Hoffmann La Roche | Ver method for the production of 2-amino-bicyclo [3.1.0] hexane-2,6-dicarboxylic acid derivatives. |
MXPA02000242A (en) | 1999-06-30 | 2004-09-10 | Prescient Neuropharma Inc | 2-aminoindane analogs. |
ATE265419T1 (en) * | 2000-05-11 | 2004-05-15 | Kenneth Curry | SPIRO(2.4)HEPTANAMINOCARBOXIC ACID AND THEREOF DERIVATIVES |
CA2411059A1 (en) | 2000-06-28 | 2002-12-06 | Taisho Pharmaceutical Co., Ltd. | Novel dicarboxylic acid derivatives |
NZ528315A (en) * | 2001-04-12 | 2005-04-29 | F | Dihydro-benzo [b] [1, 4] diazepin-2-one derivatives as MGLUR2 antagonists II |
-
2002
- 2002-12-26 AU AU2002359923A patent/AU2002359923B2/en not_active Ceased
- 2002-12-26 PT PT02793421T patent/PT1459765E/en unknown
- 2002-12-26 WO PCT/JP2002/013693 patent/WO2003061698A1/en active Application Filing
- 2002-12-26 US US10/500,101 patent/US7157594B2/en not_active Expired - Fee Related
- 2002-12-26 MX MXPA04006322A patent/MXPA04006322A/en active IP Right Grant
- 2002-12-26 KR KR1020047010069A patent/KR100897970B1/en not_active IP Right Cessation
- 2002-12-26 KR KR1020097005135A patent/KR20090031962A/en not_active Application Discontinuation
- 2002-12-26 NZ NZ533699A patent/NZ533699A/en not_active IP Right Cessation
- 2002-12-26 DK DK02793421T patent/DK1459765T3/en active
- 2002-12-26 SI SI200230736T patent/SI1459765T1/en unknown
- 2002-12-26 DE DE60228491T patent/DE60228491D1/en not_active Expired - Lifetime
- 2002-12-26 JP JP2003561641A patent/JP4230919B2/en not_active Expired - Fee Related
- 2002-12-26 AT AT02793421T patent/ATE405289T1/en active
- 2002-12-26 PL PL371014A patent/PL208123B1/en unknown
- 2002-12-26 ES ES02793421T patent/ES2311642T3/en not_active Expired - Lifetime
- 2002-12-26 EP EP02793421A patent/EP1459765B1/en not_active Expired - Lifetime
- 2002-12-26 HU HU0402649A patent/HU228436B1/en not_active IP Right Cessation
- 2002-12-26 BR BR0215462-5A patent/BR0215462A/en not_active IP Right Cessation
- 2002-12-26 CN CNB02826388XA patent/CN1281274C/en not_active Expired - Fee Related
- 2002-12-26 RU RU2004122916/15A patent/RU2315622C2/en not_active IP Right Cessation
- 2002-12-26 CA CA2471642A patent/CA2471642C/en not_active Expired - Fee Related
-
2004
- 2004-06-16 NO NO20042530A patent/NO328844B1/en not_active IP Right Cessation
- 2004-06-17 ZA ZA2004/04795A patent/ZA200404795B/en unknown
-
2005
- 2005-03-11 ZA ZA2005/02085A patent/ZA200502085B/en unknown
- 2005-07-15 HK HK05106035A patent/HK1073258A1/en not_active IP Right Cessation
-
2008
- 2008-09-29 CY CY20081101068T patent/CY1108380T1/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE405289T1 (en) | 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES | |
EP1553089A4 (en) | Antagonist of melanin-concentrating hormone receptor comprising benzimidazole derivative as active ingredient | |
DE69328856T2 (en) | Hypoglycemic dihydrochalcone derivatives | |
ATE223378T1 (en) | PROLINEAMIDE DERIVATIVES | |
WO2002010154A3 (en) | Substituted heterocyclic amides | |
AU2003246100A1 (en) | Amide derivative | |
HK1076816A1 (en) | ||
NO20061832L (en) | Carbamide derivatives of amide type | |
DK1043310T3 (en) | Biphenylamidine derivatives | |
WO2003035610A1 (en) | Sulfonamide derivative having mmp inhibitory activity | |
DE60104697D1 (en) | SULFONAMIDE DERIVATIVES | |
ATE374750T1 (en) | SEROTONIN RUPUP INHIBITORS | |
DK0978506T3 (en) | 2-phenoxyaniline | |
NO20070421L (en) | Radiosensitizing agent | |
ATE286878T1 (en) | 3,4-DIHYDRO-1H-NAPHTHALINE DERIVATIVES AS HIGHLY SELECTIVE CYCLOOXYGENASE-2 INHIBITORS | |
DE60001205D1 (en) | Azole derivatives or their salts | |
TR28240A (en) | Insecticide, nematocide and acaricide containing amidothiophosphate derivative and active inhibitor. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
UEP | Publication of translation of european patent specification |
Ref document number: 1459765 Country of ref document: EP |